Page 1
S3® MedSurg Bed
with StayPut® Frame
REF
3005
Operations Manual
2016/06 G.0 3005-009-001 REV G www.stryker.com
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Symbols
X
Warning, consult accompanying documentation
Safe Working Load Symbol
Dangerous Voltage Symbol
Alternating Current
Direct Current
Protective Earth Terminal
Potential Equalization Symbol
IPX4
Type B Equipment: equipment providing a particular degree of protection against electric shock,
particularly regarding allowable leakage current and reliability of the protective earth connection.
Class 1 Equipment: equipment in which protection against electric shock does not rely on BASIC
INSULATION only, but which includes an additional safety precaution in that means are provided
for the connection of the EQUIPMENT to the protective earth conductor in the fixed wiring of the
installation in such a way that ACCESSIBLE METAL PARTS cannot become live in the event of a
failure of the BASIC INSULATION.
Mode of Operation: Continuous
Protection from liquid splash
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock, Fire,
Mechanical and Other Specified Hazards Only in Accordance with UL 60601−1, First Edition (2003)
and CAN/CSA C22.2 No. 601.1−M90 with updates 1 and 2 and IEC 60601-1 (1998) with Amendment
1 (1991) and Amendment 2 (1995) and IEC 60601-2-38 First Edition (1996) with Amendment 1 (1999).
In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment,
this symbol indicates that the product must not be disposed of as unsorted municipal waste, but
should be collected separately. Refer to your local distributor for return and/or collection systems
available in your country.
Non-ionizing radiation; i.e. RF transmitter (WiFi)
Static Sensitive
This icon means the iBed Locator is connected.
X
This icon means the iBed Locator is not connected.
This icon means the Network is connected.
This icon means the Network is not connected.
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Table of Contents
Symbols .................................................................................3
Warning/Caution/Note Definition ...............................................................7
Introduction ..............................................................................8
Intended Use – Stryker S3® MedSurg Bed, Model 3005 ..........................................8
Intended Use – iBed® Wireless with iBed® Awareness............................................8
Expected Service Life ...................................................................9
Specifications .........................................................................9
Mattress Specifications .................................................................10
Environmental Conditions................................................................10
Product Illustration.....................................................................11
Contact Information ....................................................................12
Serial Number Location .................................................................12
Summary of Safety Precautions ..............................................................13
iBed® Wireless Option ..................................................................16
Setup .................................................................................. 17
Operation...............................................................................19
Brake Pedal Operation..................................................................19
Steer Pedal Operation ..................................................................19
CPR Emergency Release ................................................................19
Foot Prop Usage ......................................................................20
Fracture Frame Usage ..................................................................20
Foley Bag Hooks Usage .................................................................20
Patient Restraint Strap Locations ..........................................................20
Positioning Siderails....................................................................21
Control Panel Lights....................................................................21
Operating IV Poles.....................................................................22
Night Light Usage .....................................................................23
Nurse Call Backup Battery (Optional) .......................................................23
1/4 in Nurse Call Port (Optional)...........................................................23
Using the 110 Volt Outlet (Optional) ........................................................23
Nurse Control Functions (Outside Siderail) ...................................................24
Patient Control Functions Without Optional Smart TV (Inside Siderail) ...............................25
Patient Control Functions With Optional Smart TV (Inside Siderail) .................................26
Patient TV Channel Control Functions with Optional Smart TV (Inside Siderail) . . . . . . . . . . . . . . . . . . . . . . . . 27
Footboard Control Panel ................................................................28
Footboard LED Indicators ................................................................31
Display Screens.......................................................................33
Chaperone® Bed Exit (Optional) ...........................................................34
Chaperone® Bed Exit With Zone Control (Optional) .............................................35
Scale System (Optional) ................................................................36
iBed® Awareness Intended Use ...........................................................42
iBed® Awareness Functionality ............................................................42
iBed® Awareness Light Bar And Side Lights ..................................................42
iBed® Awareness ON/OFF Button..........................................................42
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Table of Contents
Footboard Operation Guide (Continued)
iBed® Awareness Monitoring and Alarms ....................................................43
Low Height .......................................................................43
Brakes...........................................................................43
Siderails .........................................................................43
Bed Exit..........................................................................44
Fowler 300+ Lock...................................................................44
Additional Alarm Conditions ...........................................................44
iBed® Awareness Locks .................................................................45
Fowler 300+ Lock button ............................................................45
Bed Motion Lock ...................................................................45
Patient Control Locks ................................................................45
Pendant - Motion/Nurse Call (3006-315-011)..................................................46
Pendant - Motion/Nurse Call/Smart Tv (Digital) (3006-315-012)....................................46
Optional Infrared (IR) Module .............................................................47
Optional iBed Locator ..................................................................48
Preventive Maintenance ....................................................................49
Checklist ............................................................................49
Cleaning................................................................................50
EMC Information..........................................................................51
Warranty ...............................................................................55
Limited Warranty ......................................................................55
Warranty Exclusion and Damage Limitations..................................................55
To Obtain Parts and Service .............................................................55
Return Authorization....................................................................55
Damaged Merchandise .................................................................55
International Warranty Clause.............................................................55
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Warning/Caution/Note Definition
The words Warning, Caution and Note carry special meanings and should be carefully reviewed.
WARNING
Alerts the reader about a situation, which if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CAUTION
Alerts the reader of a potentially hazardous situation, which if not avoided, may result in minor or moderate injury to the
user or patient or damage to the equipment or other property. This includes special care necessary for the safe and
effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or
misuse.
NOTE
This provides special information to make maintenance easier or important instructions clearer.
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Page 8
Introduction
This manual is designed to assist you with the operation or maintenance of the Stryker S3® MedSurg Bed, Model
3005. Read this manual thoroughly before operating or maintaining this product. Establish methods and procedures for
educating and training staff on the safe operation or maintenance of this product.
WARNING
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described
in this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
Notes
• This manual should be considered a permanent part of the product and should remain with the product even if the
product is subsequently sold.
• Stryker continually seeks advancements in product design and quality. Therefore, while this manual contains the
most current product information available at the time of printing, there may be minor discrepancies between your
product and this manual. If you have any questions, please contact Stryker Customer Service or Technical Support
at 1-800-327- 0770.
INTENDED USE – STRYKER S3® MEDSURG BED, MODEL 3005
The S3® MedSurg Bed, Model 3005 is intended to support and transport patients within the Med/Surg and Critical
Care hospital environments. The S3® MedSurg Bed, Model 3005 is typically used in pre-op, post-op and recovery
areas of hospital facilities. The intended user for this product is both Health Care Providers (HCPs: nurses, nurses’
aides, and medical doctors) and human patients. Lockout features may limit patient accessible controls. This product
is to be used in combination with a patient sleep surface. The bed has fowler, gatch and lift articulation capabilities,
which aide in the adjustment of surface contour, angle, and height. The product offers various options, outlined in the
product operations and maintenance manuals, including but not limited to i Bed® Awareness, scale, 110V option, IV
pole, defibrillator tray, etc. iBed® Awareness allows users to set various bed parameters to monitor bed positioning.
Chaperone® Bed Exit system alerts inform users as to patient movement within a specific zone(s) on a patient surface.
Both the iBed Awareness and Chaperone® Bed Exit system provide both visual and audible alerts. The bed may be
equipped with an integrated scale intended to weigh the patient in bed. The scale output is not intended to be used to
determine diagnosis or treatment.
The intended patient population for the S3® MedSurg Bed, Model 3005 is the following:
• The product should be used with patients upwards of 50 lb and have a maximum safe working load of 500 lb
• The patient must be at least 2 years old
• The patient must be less than 84 in without a bed extender OR 96 in with a bed extender
The product is not intended to support more than one individual at a time.
INTENDED USE – iBED® WIRELESS WITH iBED® AWARENESS
The intended use for the iBed® Wireless (with iBed® Awareness) is to assist clinical staff to monitor bed parameters
on specific Stryker beds. The desired bed parameters will be set by clinicians at the bedside. The iBed® Wireless
software is intended to be used only with specifically enabled Stryker beds that have been verified and validated with
the i Bed® Wireless software, and is not intended to provide bed status information for non-Stryker beds. The iBed®
Wireless software is not intended to communicate any patient status information, nor to permanently store any type
of data. The iBed® Wireless with iBed® Awareness System is not intended to provide automated treatment decisions
or as a substitute for professional healthcare judgment. The iBed® Wireless with iBed® Awareness System is not a
replacement or substitute for vital signs monitoring or alert equipment. All patient medical diagnosis and treatment are
to be performed under direct supervision and oversight of an appropriate health care professional.
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Page 9
Introduction
EXPECTED SERVICE LIFE
The S3® MedSurg Bed, Model 3005 has an expected service life of 10 years under normal use conditions and with
appropriate periodic maintenance as described in the maintenance manual for each device.
SPECIFICATIONS
Safe Working Load
Note: Safe Working Load indicates the sum of the
patient, mattress, and accessory weight.
Bed Weight 570 lb 259 kg
Scale System Capacity (optional equipment). Loads weighing
up to
± 3 pounds for patients weighing 50 to 100 pounds
Scale System Accuracy (optional equipment)
Overall Length/Width
Patient Sleep Surface 84 in x 35 in 213.4 cm x 88.9 cm
Bed Height to Top of Seat Litter - 6 in Casters 16 in to 30 in ±0.5 40.6 cm to 76.2 cm
Litter Platform
to Top of
Siderail
Space Between Siderails (Full Up) 2-1/4 in 5.72 cm
Knee Gatch Angle 0° to 40°
Fowler Angle 0° to 60° (±5° at all angles except 30°, ±3° at 30°)
Trendelenburg/Reverse Trendelenburg +12° (+1°/-2°) to -10° (± 1°)
Electrical Requirements - all electrical requirements meet
UL 60601 specifications.
iBed® Wireless (option)
Outlet Option 110VAC, 60 Hz, 10A
Duty Cycle 1 minute 45 seconds ON, 30 minutes OFF
StayPut® Bed Frame Technology
Full Up Head End Siderail 15 i n 38.1 cm
Full Up Foot End Siderail 15 -1/2 i n 39.37 cm
Siderails Up 93 in x 41-1/2 in 236.2 cm x 105.41 cm
Siderails Down 93 in x 39-1/2 in 236.2 cm x 100.3 cm
± 3% of the total patient weight for patients weighing
100 to 500 pounds
120VAC, 60Hz, 8A
802.11 b/g, 2.4 GHz
• Minimum Operational Signal Strength: -65 dB
• Supported Securities:
• Supports IPv4 and DHCPv4
802 .1x
• MS-CHAPv2
Maintains the relative location of the patient when
the head of the bed is raised. This helps reduce
the need for patient repositioning once the bed
adjustment is made. Patients also remain in close
proximity to bedside belongings as the bed is
articulated.
500 lb 227 kg
500 lb 227 kg
WEP
WPA-PSK (TKIP)
WPA 2- PS K (CCMP/AES)
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Page 10
Introduction
MATTRESS SPECIFICATIONS
Thickness 6 in 15. 2 cm
Width >= 35 in >= 88.9 cm
Length >= 84 in >= 213.4 cm
ILD 80 lb 36.3 kg
The above stated mattress specifications assist in ensuring the product conforms to HBSW and IEC specifications.
ENVIRONMENTAL CONDITIONS
Environmental Conditions Operation Storage and Transportation
Ambient Temperature
50 0F
(10
0
F
104
0
C)
(40
0
C)
-22 0F
(-30
0
C)
140
(60
0
F
0
C)
75%
95%
Relative Humidity
(Non-Condensing)
30%
1060 hPa
10%
1060 hPa
Atmospheric Pressure
700 hPa
500 hPa
Stryker reserves the right to change specifications without notice.
Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.
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Page 11
PRODUCT ILLUSTRATION
Introduction
Control Panel
Steer
Pedal
(no t
shown)
Nurse
Ground Chain
Headboard
Siderail Release
Handle
Brake
Pedal
Patient
Control Panel
Siderail
Footboard
Control Panel
Caster
Ground Chain
Footboard
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Page 12
Introduction
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, Michigan 49002
USA
Please have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical
Support. Include the serial number in all written communication.
SERIAL NUMBER LOCATION
The serial number is located at the head end of the
bed just below the headboard and above the power
cord where it comes out from the frame.
Head End of Bed
R
REF
A
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SN
This product is protected by the following U.S . patents , and other patents pending:
US 5172442
3005S3
Serial No.
Date of Mfg.
120V~60Hz, 8A
MAX .
500 lbs. [227 Kg.]
WAR NING: Does not tolerate mac hine was hing or jet wash!
R ated Duty C ycle: 1min. 45 s ec. O n / 30 min. Off
Stryker Medical - Portage, MI 49002-5826
US 5 276432 US 5 329657 US 5 343581
87VL
MEDICAL
ELECTRICAL
EQUIPMENT
UL 60601-1
CAN/CSA C22.2
NO. 601.1
Made in U.S.A.
Page 13
Summary of Safety Precautions
Carefully read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described
in this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
• Always operate the product when all operators are clear of the mechanisms.
• Always allow the product to reach room temperature before conducting any setup or testing functional operations
to prevent permanent product damage.
• Danger: Explosion hazard. Do not use in the presence of flammable anesthetics.
• Always apply the brakes when a patient is getting in the product or out of the product to avoid instability.
• Always apply the brakes when the patient is unattended.
• Always make sure that the brakes are completely released prior to moving the product. Attempting to move the unit
with the brakes actuated could result in injury to the user and/or patient.
• Do not attempt to move the product laterally after you apply the steer lock pedal. The product cannot swivel when
transporting with steer lock.
• Always make sure that all persons and equipment are away from the area below and around the fowler before you
activate the CPR release. The CPR release is for emergency use only.
• Always lock the siderails in the full up position with the sleep surface horizontal in the lowest position when the
patient is unattended.
• Always lock the siderails in the full up position with the sleep surface horizontal in the lowest position when
transferring a patient.
• Always lock the siderails unless a patient’s condition requires extra safety measures.
• Do not use the intermediate position in place of the highest position.
• Always use a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly,
which may result in patient or user injury.
• Always plug the product directly into a properly grounded, three-prong receptacle. You can only achieve grounding
reliability when you use a hospital-grade receptacle. This product is equipped with a hospital-grade plug for
protection against electric shock hazard.
• Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by
equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not
exceed 300 microamps. Grounding continuity should be checked periodically.
• Do not use the optional 110V outlet for life sustaining equipment.
• Do not route cords between a support surface and the product.
• Do not attach power cords to any moving part of the product.
• Do not use siderails as restraint devices to keep the patient from exiting the product. The design of the siderails
keep the patient from rolling off the product. The operator must determine the degree of restraint necessary to
make sure that the patient is safe. Failure to use the siderails as intended could result in serious patient injury.
• Do not use Bed exit (optional) to replace patient monitoring protocol.
• Do not use iBed Awareness (optional) as a lock indicator for siderails.
• Do not use iBed Awareness (optional) to replace patient monitoring protocol.
• Do not use the iBed Awareness LED light bars (optional) to replace patient monitoring protocol.
• Always make sure that the siderails are locked before you arm iBed Awareness.
• Do not turn off the iBed Awareness alarm. You will lose access to the event manager that displays the compromised
parameter condition.
• Always unplug the bed power cord from the wall socket and push the battery power on/off switch to the “OFF”
position (if applicable) before servicing or cleaning the bed. When working under a bed in the high position, always
place blocks under the litter frame and apply the brakes to prevent injury in case the Bed Down switch is accidently
pressed.
• Always unplug all power cords before opening the service compartment, junction box, or receptacle to avoid the risk
of electrical shock.
• Always secure the foot prop during cleaning or servicing.
• Always place the IV pole in the upright position before using the drive handle to avoid pinching your fingers.
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Page 14
Summary of Safety Precautions
WARNING (CONTINUED)
• Always use extra supervision when using a mattress or support surface thicker than six in. (15,4 cm).
• When a patient’s condition (such as disorientation due to medication or clinical condition) could lead to patient
entrapment, the mattress support platform should be left in the flat position while the patient is unattended (except
when required otherwise my medical staff for special or particular circumstances).
• Trendelenburg is not easily achievable when mains voltage has been interrupted.
• Medical electrical equipment (i.e. Optional Scale System) requires special precautions regarding EMC and needs
to be installed and put into service according to the EMC information to prevent equipment malfunction.
• Portable and mobile RF communication equipment can affect Medical Electrical Equipment (i.e. Optional Scale
System).
• Do not use the scale system readings as the only reference for medical treatment.
• Shock hazard: Improper handling of the power cord may result in damage to the power cord and potential shock
hazards. If damage has occurred to the power cord, immediately remove the bed from service and contact the
appropriate maintenance personnel. Failure to do so could result in serious injury or death.
• To avoid malfunction, the scale system (optional) should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the Optional Scale System should be observed to verify normal operation
in the configuration in which it will be used.
• Confirm proper scale system operation following mattress installation. For best results, secure the therapy mattress
power cord to prevent damage to the cord or interference with the bed frame and the scale system.
• Do not set the scale to zero when support surface therapies are active. The motion from the support surface
therapies may adversely affect bed exit system performance.
• Do not arm bed exit when support surface therapies are active. The motion from the support surface therapies
may adversely affect bed exit system performance.
• Always determine the proper use of the restraint straps and restraint strap locations. Improperly adjusted restraint
straps can cause serious injury to a patient. Stryker is not responsible for the type or use of restraint straps on any
of Stryker’s products.
CAUTION
• Power save mode activates after one hour on battery power with no motion release switch activation. Bed exit,
scale, and product motion stops operating when the product enters the power save mode.
• Always raise the siderails when you lower the litter to its lowest position to prevent interference with the scale
system.
• Always make sure that you set the desired product parameters before you enable iBed Awareness.
• Do not use accessories that cover the footboard and outside siderail LED light bars.
• Do not use accessories that cover the control panels or mechanical parts of the product.
• Do not turn off the iBed Awareness alarm. You will lose access to the event manager that displays the compromised
parameter condition.
• Always unplug the power cord during service or cleaning.
• When large spills occur in the area of the circuit boards, 120 volt cables and motors, immediately unplug the bed
power cord from the wall socket. Remove the patient from the bed and clean up the fluid. Have maintenance completely check the bed. Fluids can affect the operational capabilities of any electrical product. DO NOT put the bed
back into service until it is completely dry and has been thoroughly tested for safe operation.
• Preventative maintenance should be performed at a minimum of annually to ensure all bed features are functioning
properly. Close attention should be gi ven to safety features including, but not limited to, safety side latching mechanisms,
frayed electrical cords and components, all electrical controls returning to the off or neutral position when released,
caster braking systems, no controls or cabling entangled in bed mechanisms, leakage current 300 μA (microamps)
maximum, scale and bed exit systems calibrated properly, and the siderail gas spring not leaking oil.
• Do not move footboards from one product to another. Individual products may have different options. Mixing
footboards could result in unpredictable operation of the product.
• The lockout buttons on the footboard lock the Fowler, Gatch and Bed Up/Down functions and prevent motion of the
bed. It is the responsibility of attending medical personnel to determine whether these functions should be locked
and to use the buttons accordingly.
• The maximum safe working load for each IV pole is 40 pounds.
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Page 15
Summary of Safety Precautions
CAUTION (CONTINUED)
• Do not use IV poles push/pull device.
• To reduce the risk of electric shock hazard, the caregiver shall exercise caution not to touch the patient and the
load cell connector or pendant port connector at the same time.
• Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse
Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the
potential for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full
down position to prevent the interference from causing the scale system to weigh inaccurately.
• The use of a mattress overlay may reduce the effectiveness of the siderail.
• The cleanliness and integrity of both ground chains must be maintained to minimize static build up and discharge.
Make sure that the ground chains are in place, intact and touching the floor.
• Do not add or remove weight when the bed exit system is armed.
• There is a possible fire hazard when using half bed length type oxygen administering equipment. Ensure the
siderails are outside of the tent.
• There is a possible fire hazard when used with oxygen administering equipment of other than the nasal or mask
type. Lock the control at foot of bed when using oxygen administering equipment.
• The weight of the foley bags placed on isolated bag hooks should not exceed five pounds.
• The weight of pumps placed on footboard pump holder should not exceed 45 pounds.
• The safe working load of the defibrillator tray is 40 lb.
• The safe working load of the oxygen holder is 45 lb.
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Page 16
Summary of Safety Precautions
iBED® WIRELESS OPTION
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the iBed® Wireless option.
WARNING
• The optional iBed® Wireless function provides remote information of bedside information to aid the caregiver. In
no way does this option replace the caregiver’s responsibility of checking on patients. Caregivers should not rely
only on the remote information to perform their duties.
• The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate
location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote
information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be remapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the
room / location information is changed after initial installation.
• Line of sight between iBed Locator and the head end of bed must be free of obstruction at all times. Any line
of sight interference could impede communication and cause the room / location information not to be available.
• iBed® Wireless compatible footboard must be used for all iBed® Wireless beds. Some iBed® Wireless functionality
will be lost if an older version of the footboard is used.
• iBed® Wireless functionality shall be verified after installation. Failure to do may result loss of remote information
or wrong remote information. At a minimum, verify i Bed locator communication with bed in all bed positions, and
iBed® Wireless communication with the wireless access point.
• iBed Locators must be installed more than 71” apart from one another in the same room, such as in a semi-private
room with more than one bed. Failure to do so could result in a bed communicating with the other adjacent iBed
Locator, thus providing incorrect bed location information.
CAUTION
Wireless bed only transmits bed information and not nurse call information. The wireless bed is not intended to replace
the existing nurse call system.
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Page 17
Setup
It is important that the S3® MedSurg Bed, Model 3005 is working properly before it is put into service. The following
list will help ensure that each part of the bed is tested.
WARNING
• Always plug the product directly into a properly grounded, three-prong receptacle. You can only achieve grounding
reliability when you use a hospital-grade receptacle. This product is equipped with a hospital-grade plug for
protection against electric shock hazard.
• Always use a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly,
which may result in patient or user injury.
1. Plug the bed into a properly grounded, hospital grade wall receptacle and ensure the power button LED light at
the foot end of the bed comes on.
2. Plug the optional interface cable into the 37-pin connector under the litter frame at the head end of the bed, into
the “Patient Station”, “Head Wall”, “Docker Station” or equivalent (whichever applies). Test the interface cable to
verify it is functioning properly.
3. Ensure the siderails raise, lower, lock in the up position, lock in the intermediate position when lowered and store
smoothly (see page 21).
4. Ensure that all four casters lock when the brake pedal is engaged (see page 19).
5. Raise the fowler (head of bed) up to approximately 600. Squeeze the CPR release handle and ensure the back
will drop with minimal effort.
NOTE
Ensure that the “Brake” LED located on the outside of the head end siderails and on the footboard control panel
blink when the brakes are not engaged.
6. Perform each function on the footboard control panel to ensure that each function is working properly (see page
29).
7. Perform each function on both head end siderails to ensure that each is working properly (see page 21).
8. Activate the motion stop system to ensure it is functioning properly; press the BED DOWN button to lower the
bed. As the bed lowers, push up on the motion interrupt pan under the bed and ensure the downward motion
stops. Release the pan and allow the downward motion to continue.
NOTE
The bed’s upward motion or other functions are not disrupted by the motion stop system.
9. If the bed is equipped with the Nurse Call option, verify it is functioning properly prior to patient use.
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Page 18
Setup
iBED® WIRELESS OPTION
In order for your bed to be capable of receiving a wireless connection the iBed Locator needs to be installed on the
wall at the head end of the bed. The iBed Locator communicates with the IR Module installed in your bed. For detailed
instructions on mounting the 5212 i Bed Locator refer to the instruction sheet (part number 5212-009-101) packaged
with your optional 5212 iBed Locator Installation kit.
If any problems are found during the iBed Locator Installation, contact Stryker Technical Support at (800) 327−0770.
WARNING
The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate location
information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote information.
Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be re-mapped to the new
room / location in which it is moved to. iBed Locator re-mapping will also be required if the room / location information
is changed after initial installation.
The wireless connection settings need to be loaded before the device will communicate with the iBed Server application.
Reference the iBed Server Installation and Configuration Manual (5212-009-001).
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Page 19
Operation
BRAKE PEDAL OPERATION
WARNING
Always apply the caster brakes when a patient is getting on or off the bed. Push the bed sideways to ensure the brakes
are securely locked. Always engage the brakes unless the bed is being moved. Injury could result if the bed moves
while a patient is getting on or off the bed.
To activate the brakes, push down once on one of the pedals
located at the midpoint of the bed on both sides (identified by
the label at right). The pedal will remain in the lowered position,
indicating the brakes are engaged. To disengage the brakes,
push down once and the pedal will return to the upper position.
NOTE
The LED lights located on the outside of the head end siderails and on the foot end control panel will blink when the
brakes are not engaged only if the bed is plugged into a wall socket or is running on battery power (see page 24 &
page 31. The brakes will still operate properly when the bed is not plugged in.
STEER PEDAL OPERATION
When the bed is moved, the steer caster helps guide the bed along a straight line and helps the bed pivot around
corners.
To activate the steer caster, move the pedal located at the head
end of the bed to your right as shown on the label.
NOTE
For proper “tracking” of the steer caster, push the bed approximately 10 feet to allow the wheels to face the direction of
travel before engaging the steer pedal. If this is not done, proper “tracking” will not occur and the bed will be difficult
to steer.
WARNING
Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal is
activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when the steer
pedal is activated may cause injury to the user.
CPR EMERGENCY RELEASE
When quick access to the patient is needed, and the Fowler (head of bed) is raised, squeeze one of the two release
handles (marked by the red CPR label) and the fowler can quickly be guided down to a flat position.
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Page 20
FOOT PROP USAGE
Operation
The foot prop causes the foot end of the Knee Gatch to rise
when the Gatch button is used to raise the Gatch. To lower
the foot end of the Gatch, release the prop by grasping the
end of the Knee Gatch, lifting upward and swinging the prop
(A) toward the head end of the bed which will disengage the
prop stop.
WARNING
Always secure the foot prop during cleaning or servicing.
CAUTION
Do not place objects or apply weight to the foot end cover.
This is a protective cover only.
FRACTURE FRAME USAGE
A standard fracture frame can be mounted on the bed using
the I.V. sockets located on all four corners of the bed. I.V.
poles can be used in conjunction with a fracture frame if the
I.V. pole adaptor sockets are purchased.
Lift up Knee Gatch
Head End
Foot End
A
WARNING
Use only retractable traction or fracture frames. Failure to
use a retractable frame may result in injury to the patient
and/or damage to the equipment.
Foot End Cover
FOLEY BAG HOOKS USAGE
The standard foley bag hooks are found at four locations (on each side of the bed); below the seat (middle) section
and at the extreme foot end of the frame. Optional isolated foley bag hooks can be purchased and are located at the
foot end of the bed under the frame. The patient weight reading on the scale system is not affected when the optional
isolated foley bag hooks are used.
PATIENT RESTRAINT STRAP LOCATIONS
The bed has 10 locations for installing patient restraint straps on the litter top, five on each side of the bed.
WARNING
Always determine the proper use of the restraint straps and restraint strap locations. Improperly adjusted restraint straps
can cause serious injury to a patient. Stryker is not responsible for the type or use of restraint straps on any of Stryker’s
products.
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Page 21
Operation
POSITIONING SIDERAILS
• The siderails can be locked at two heights (intermediate & full up).
• The siderails can slide in towards the bed when not in use. To remove the rail from the tucked position, grasp the
top of the rail and pull outward.
• To raise head end siderail to full height position, grasp the rail and swing it upward until it locks in place (two clicks
are heard).
NOTE: When the siderail is being raised, it does not lock in the intermediate position unless it is
brought back after the first click.
• To lower the siderail and lock in intermediate position, pull outward on the siderail release handle (A) and rotate
the siderail down toward the head end of the bed until it locks at the intermediate position.
• To lower the siderail in its full down position, pull outward on the release handle (A) and rotate the siderail
downward toward the head end of the bed until it is completely lowered.
• To raise and lower the foot end siderail, the same procedures are required as for the head end siderail, however,
the siderail swings toward the foot end of the bed.
WARNING
• Do not use siderails as restraint devices to
keep the patient from exiting the product. The
design of the siderails keep the patient from
rolling off the product. The operator must
determine the degree of restraint necessary
to make sure that the patient is safe. Failure
to use the siderails as intended could result in
serious patient injury.
• Always lock the siderails in the full up position
with the sleep surface horizontal in the lowest
position when the patient is unattended.
• Always lock the siderails in the full up position
with the sleep surface horizontal in the lowest
position when transferring a patient.
• Always lock the siderails unless a patient’s
condition requires extra safety measures.
A
To disengage the rail, pull outward on release handle (A) and swing the rail down to the desired height (intermediate
or full down). When storing siderails, ensure they are at a full down position.
CONTROL PANEL LIGHTS
The bed is equipped with lights to illuminate the head end siderail control panel and the red nurse call switches.
Both can be activated at the footboard control panel. Five settings are available for the control panel lights: Off, Low
Intensity, Medium Intensity, High Intensity and Nurse Call Only.
To change the control panel light settings, press the “Menu” button on the footboard. Scroll down through the
menu items and select “Backlight” then press “Enter”. Select the desired setting by highlighting it and then pressing
“En ter ”.
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Page 22
Operation
OPERATING IV POLES
WARNING
Always place the IV pole in the upright position before using the drive
handle to avoid pinching your fingers.
To use the Removable IV pole:
1. Install the pole at any of the four receptacles on the bed top (located
on all four corners of the frame).
2. To raise the height of the pole, turn knob (A) counterclockwise and
pull up on the telescoping portion (B) of the pole and raise it to the
desired height.
3. Turn knob (A) clockwise to tighten the telescoping portion in place.
CAUTION
The maximum safe working load for each IV pole is 40 pounds.
To use the 2-Stage Permanently Attached IV pole:
NOTE
The 2-stage permanently attached IV pole is an option and may have been
installed at either the head, foot or both ends of the bed. The choice was made
at the time the unit was purchased.
1. Lift and pivot the pole from the storage position and push down until it
rests in the receptacle.
2. To raise the height of the pole, pull up on the telescoping portion (A) until
it locks into place at its fully raised position.
3. Rotate the IV hangers (B) to desired position and hang IV bags.
4. To lower the IV pole turn the latch (C) clockwise until section (A) lowers.
A
C
B
CAUTION
The maximum safe working load for each IV pole is 40 pounds.
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Page 23
Operation
NIGHT LIGHT USAGE
The bed is equipped with two night lights to illuminate the floor area around the bed. There is a switch under the litter
thigh section on the patient’s left side that turns both lights on and off.
WARNING
Service only by qualified personnel. Refer to the maintenance manual. Verify the power cord is unplugged before
servicing.
NURSE CALL BACKUP BATTERY (OPTIONAL)
• To prevent a low battery condition when the bed is not plugged
in, position the cord out switch at the head end of the bed to the
off position. The switch is identified by the label shown below. If
the switch is not positioned as shown below and the bed power
cord and pendant cord are unplugged, the life of the backup
battery will be significantly reduced.
• If the Nurse Call battery needs to be replaced, a message will appear on the footboard display. The battery is
located on the patient’s left side at the head end of the bed. No tools are required to replace the battery. Unplug
the bed power cord from the wall socket and remove the battery from its housing to replace.
1/4 IN NURSE CALL PORT (OPTIONAL)
• The optional ¼ in nurse call port is only designed to function with nurse call cords that have a ¼ in TS connector.
• Fully insert the attached dummy plug into the port whenever a nurse call cord is not inserted into the port.
• If a continuous nurse call signal is observed, ensure that the dummy plug or a compatible nurse call cord is fully
inserted into the port.
USING THE 110 VOLT OUTLET (OPTIONAL)
• The 110V outlet has its own power cord that must be plugged into a properly grounded hospital grade three prong
wall receptacle different from the wall receptacle the bed power cord is plugged into.
• If the equipment plugged into the bed outlet is not receiving power, check the 10A circuit breakers located on the
litter frame under the head section. Reset, if necessary.
WARNING
• Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by
equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not
exceed 300 microamps. Grounding continuity should be checked periodically.
• Do not use the optional 110V outlet for life sustaining equipment.
• Do not route cords between a support surface and the product.
• Do not attach power cords to any moving part of the product.
• Always unplug all power cords before opening the service compartment, junction box, or receptacle to avoid the risk
of electrical shock.
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Page 24
Operation
NURSE CONTROL FUNCTIONS (OUTSIDE SIDERAIL)
3
6
8
1
7
92 4 5
LEFT OUTER SIDERAIL SHOWN
(RightOuterSiderailsameastheLeft)
Button Button Name Button Function
Brake LED
1
Cardiac Chair
2
Bed/Litter Up Press to raise the Bed/Litter.
3
Bed/Litter Down Press to lower the Bed/Litter.
4
Nurse Call Push to activate Nurse Call.
5
Knee Gatch Up Press to raise the Knee Gatch.
6
Knee Gatch Down Press to lower the Knee Gatch.
7
Fowler Up Press to raise the Fowler.
8
Fowler Down Press to lower the Fowler.
9
LED flashes when Brakes are not engaged.
LED is “Off” when brakes are engaged.
Press to activate the Cardiac Chair function.
• The Knee will raise.
• The back will raise to approximately 60
• The bed will tilt to approximately −100 reverse
Trendelenburg (foot end down).
0
NOTE: The intent of the nurse call light on the siderails is to ensure the patient immediately knows which button to
push to contact the nurse station. Turning the light off may compromise this ability, especially in a darkened room.
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Page 25
Operation
PATIENT CONTROL FUNCTIONS WITHOUT OPTIONAL SMART TV (INSIDE SIDERAIL)
1
8
9
12
2
3
5
6
7
LEFT INSIDE SIDERAIL SHOWN
(RightInsideSiderailsameastheLeftwithexceptionoftheNurseCallandNurse
AnswerLED.LED7and8willchangepositionsontherightinnersiderail)
10
114
Button Button Name Button Function
TV On/Off Press to turn TV or radio on and to select a channel.
1
Room Light Press to turn the room light On/Off.
2
Bed Overhead Light Press to turn the bed overhead light On/Off.
3
TV/Radio Volume Down Press to decrease volume; TV or Radio.
4
TV/Radio Volume Up Press to increase volume; TV or Radio.
5
Press to activate Nurse Call.
10
11
12
Nurse Call
6
Nurse Call LED
7
Nurse Call Answer LED Illuminates green when answered by Nurse.
8
Fowler Up Press to raise the Fowler.
9
Fowler Down Press to lower the Fowler.
Knee Gatch Down Press to lower the Knee Gatch.
Knee Gatch Up Press to raise the Knee Gatch.
NOTE: Yellow LED will light when button is pushed.
Green LED will light with Nurse Station acknowledgment.
Illuminates amber when nurse call has been pressed by
patient.
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Page 26
Operation
PATIENT CONTROL FUNCTIONS WITH OPTIONAL SMART TV (INSIDE SIDERAIL)
1
8
9
12
2
3
5 6
10
114 7
LEFT INSIDE SIDERAIL SHOWN
(RightInsideSiderailsameastheLeft)
Button Button Name Button Function
TV On/Off Press to turn TV or radio on and to select a channel.
1
Room Light Press to turn the room light On/Off.
2
Bed Overhead Light Press to turn the bed overhead light On/Off.
3
TV Volume Down Press to decrease TV volume.
4
TV Volume Up Press to increase TV volume.
5
Press to activate Nurse Call.
10
11
Nurse Call
6
Nurse Call LED
7
Nurse Call Answer LED Illuminates green when answered by Nurse.
8
Fowler Up Press to raise the Fowler.
9
Fowler Down Press to lower the Fowler.
Knee Gatch Down Press to lower the Knee Gatch.
NOTE: Yellow LED will light when button is pushed.
Green LED will light with Nurse Station acknowledgment.
Illuminates amber when nurse call has been pressed by
patient.
12
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Knee Gatch Up Press to raise the Knee Gatch.
Page 27
Operation
PATIENT TV CHANNEL CONTROL FUNCTIONS WITH OPTIONAL SMART TV (INSIDE SIDERAIL)
1
2
LEFT INSIDE SIDERAIL SHOWN
(RightInsideSiderailsameastheLeft)
Button Button Name Button Function
TV Channel Up Press to change TV channel up.
1
3
4
TV Channel Down Press to change TV channel down.
2
Mute TV
3
Closed Caption
4
www.stryker.com 3005-009-001 REV G 27
Press to mute TV volume.
Press again to turn the sound back on.
Press to display the closed captioning.
Press again to turn off the closed captioning.
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Page 28
FOOTBOARD CONTROL PANEL
Operation
1715 16
SCALE
181920
iBED / MENU
21
LOCKS
2
1
4
6
73 5 9 13
MOTION
8 101112
BED EXIT
14
Button Name Button Name Button Name
Bed Motion Lock 9 Bed/Litter Down 18 Scale
1
22 24
2523
Fowler 300+ 10 Fowler Up 19 Scale Zero
2
Patient Fowler Lock 11 Fowler Down 20 iBed On/Off
3
Patient Gatch Lock 12 Knee Gatch Up 21 Menu
4
Patient Bed Up/
5
Down Lock
Trend 14 Cardiac Chair 23 Menu Down
6
Reverse Trend 15 CPR Drop 24 Exit
7
Bed/Litter Up 16 Bed Exit Arm/Disarm 25 Enter
8
13 Knee Gatch Down 22 Menu Up
17 Bed Exit Zone Control
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Page 29
Operation
FOOTBOARD CONTROL PANEL (CONTINUED)
2
8
10
Button Name Function
Bed Motion Lock
1
Fowler 300+
2
Patient Fowler Lock
3
LOCKS
Patient Gatch Lock
4
Patient Bed
5
Up/Down Lock
Trendelenburg Lowers head end and raises foot end of bed.
6
Reverse
7
Trendelenburg
Bed/Litter Up Raises Bed/Litter.
8
Bed/Litter Down Lowers Bed/Litter.
9
Fowler Up Raises Fowler.
10
Fowler Down Lowers Fowler.
11
Knee Gatch Up Raises Knee Gatch.
12
Knee Gatch Down Lowers Knee Gatch.
13
MOTION
Cardiac Chair
14
CPR Drop
15
126 14
111 4 73 5 9 13 15
Locks all motion on bed. The Bed Motion Lock button will illuminate when
activated.
Moves bed out of trend and raises the Fowler to 300. The Fowler 300 +
button and LED light will illuminate when activated. NOTE: The Fowler will
not go below 300 once the Fowler 300+ lock is activated. However, it may
be raised or lowered in the 300 to 600 range.
Locks out Fowler control at all locations (Siderail, Pendant, Head End) with
the exception of the operator controls located on the Footboard. The Patient
Fowler Lock button will illuminate when activated.
Locks out Gatch control at all locations (Siderail, Pendant, Head End).
The Patient Gatch Lock button will illuminate when activated. This function
also prevents the auto contour of the Gatch when motion is used. NOTE:
Auto contour is the feature of the bed that when fowler is actuated, Gatch
automatically moves with the Fowler.
Locks out Bed Height control at all locations (Siderail, Pendant, Head End)
with the exception of the operator controls located on the Footboard. The
Patient Bed Up/Down Lock button and Bed Motion LED lights will illuminate
when activated.
Lowers foot end and raises head end of bed
When activated, the knee will raise, the Fowler will raise or lower to
approximately 600 degrees and the bed will tilt to approximately -100 Reverse
Trendelenburg (foot end down).
Activates electronic CPR function; flattens litter and puts bed in low
height.
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Page 30
Operation
FOOTBOARD CONTROL PANEL (CONTINUED)
Button Name Function
Bed Exit Arm/Disarm
16
Zone Control Changes the Zone.
17
BED EXIT
181920
1716
Activates Bed Exit system. The selected zone graphic will illuminate
when activated. When Bed Exit is in alarm mode, press and hold
“Arm/Disarm” to turn Bed Exit “Off”.
21
22 24
2523
SCALE
iBED/MENU
Scale Displays scale information on screen.
18
Zero Zeroes Bed.
19
On/Off Tur n s iBed® Awareness system ON/OFF.
20
Menu Accesses MENU selections.
21
Menu Up Scroll Up through menu.
22
Menu Down Scroll Down through menu.
23
Exit
24
Enter Selects menu item; also used to Save operations.
25
Exits or Escapes from menu selection; also used to Cancel
operations.
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Page 31
Operation
FOOTBOARD LED INDICATORS
The LED indicators on the footboard control panel illuminate when there is a parameter change on the product.
H
B
F
G
A
DC E
LED Name: Function LED Color
Bed Motion Lock LED: LED is illuminated if Bed Motion is locked; blinking if
A
motion is attempted when lock is “On”.
Fowler 300+ Lock LED: LED is illuminated if Fowler 300+ is locked; blinking if
locked and Fowler motion is attempted while Fowler is at 300; flashes if lock
B
condition is violated by CPR.
Patient Control Fowler Lock LED: LED is illuminated if the Patient Fowler Lock
C
is “On”.
Patient Control Gatch Lock LED: LED is illuminated if the Patient Gatch Lock
D
is “On”.
Patient Control Bed Up/Down Lock LED: LED is illuminated if the Patient Bed
E
Up/Down Lock is “On”.
Zone 1 LED: LED is illuminated when Bed Exit is “On” and Zone 1 activated;
F
flashes if a Bed Exit event occurs.
Zone 2 LED: LED is illuminated when Bed Exit is “On” and Zone 2 activated;
G
flashes if a Bed Exit event occurs.
Zone 3 LED: LED is illuminated when Bed Exit is “On” and Zone 3 activated;
H
flashes if a Bed Exit event occurs.
AMBER
AMBER
AMBER
AMBER
AMBER
AMBER
AMBER
AMBER
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Page 32
Operation
FOOTBOARD LED INDICATORS (CONTINUED)
A
B
C
D
E F G
Optional
LED Name: Function LED Color
Bed Motion Lock LED: LED is illuminated when Bed Motion Lock is activated
or when the Patient Control (Fowler, Gatch, Bed Up/Down) Lock buttons are
A
activated.
Fowler 300+ LED: LED is illuminated when the Fowler 30+ is locked. The
LED will blink if the iBed® Awareness system is “On”, the Fowler 30+ is being
B
monitored and the Fowler goes below 30 degrees or the Fowler 30+ is turned
“O f f”.
Low Height LED: LED is illuminated when bed is in low height. The LED will
blink if the iBed® Awareness system is “On”, the low height is being monitored,
C
and the bed is not in low height.
Brake LED: LED is illuminated when the brake is set, and will blink if the brake
D
is not set.
Bed Exit LED (Optional): LED is illuminated when the Bed Exit is armed. The
LED will blink if the Bed Exit is turned Off while the i Bed® Awareness system is
E
turned On or if Bed Exit alarms while monitored by iBed® Awareness system.
Bed Zero LED (Optional iBed® Awareness): LED is illuminated if Bed Zero is
F
successful.
Siderail LED (Optional iBed® Awareness): LED is illuminated if iBed® Awareness
G
system is “On”. The LED will blink when siderail state has changed.
Power LED: LED is illuminated when bed has power. GREEN
H
AMBER
AMBER
AMBER
AMBER
AMBER
AMBER
AMBER
H
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Page 33
X
Operation
DISPLAY SCREENS
There are four types of display screens listed by priority below with one being the highest.
Screen Type Priority
Bed Exit Alarm Message
Alarm Indications
Brake Alarm Message
iBed® Awareness Alert Messages
Messages
Conditional Message
Menus Main Menu
Status Screen Default Screen
A. Power Up
• The initialization screen shown in Figure 1 will be displayed
on power up.
B. Status Screen (without iBed® Wireless option)
• Figure 2a shows an example of the default “Status” Screen.
• Information on this screen includes the ‘Fowler Angle’ and the
‘Trend Angle’ values.
• If this screen is inactive for 60 seconds, the Backlighting will
be reduced.
C. Status Screen (with iBed® Wireless option)
• Figure 2b shows an example of the default “Status” Screen.
• Information on this screen includes the WiFi and iBed Locator
connection status, ‘Fowler Angle’ and ‘Trend Angle’ values.
• If this screen is inactive for 60 seconds, the Backlighting will
be reduced.
23
1
2
3
4
5
6
Figure 1
0
-12
0
Icons
Wireless
Connectivity
Status
Signal
Strength Level
Signal
Strength, X
D. Message Screen
• As required message screens are provided during alarm conditions and user interaction with the bed.
E. Main Menu
• The Menu screen provides of list of available features accessible to the operator.
www.stryker.com 3005-009-001 REV G 33
Not
Connected;
Trying to
Connect
None Low Good Excellent
X < -90
dB or
X = 0 dB
-90 dB ≤
X < -71 dB
Connected
-71 dB ≤
X < -57 dB
X ≥ -57 dB
23
0
Figure 2a
300.6lbs
Figure 2b
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-12
0
Page 34
Operation
CHAPERONE® BED EXIT (OPTIONAL)
“Bed Exit” LED
1. Before positioning the patient on the bed, the scale system must be zeroed for the Bed Exit System to function
properly (see page 37 for instructions on zeroing the scale system).
2. Position the patient on the bed and press the “Arm/Disarm” button to activate the Bed Exit function. The footboard
“Bed Exit” LED and indicator “Bed Exit” LED will turn on.
3. To deactivate Bed Exit, press the “Arm/Disarm” button. The footboard “Bed Exit” LED and the indicator “Bed Exit”
LED will turn off.
NOTE
Moving the litter position after Bed Exit is armed may trigger the alarm.
WARNING
The Bed Exit System is intended only to aid in the detection of a patient exiting the bed. It is NOT intended to replace
patient monitoring protocol. It signals when a patient is about to exit. Adding or subtracting objects from the bed after
arming the bed exit system may cause a reduction in the sensitivity of the bed exit system. To avoid possible injury and
to assure proper operation when using a powered mattress replacement system such as XPRT, do not initialize (“Arm”)
bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and position resulting from a
dynamic therapy mattress may adversely affect bed exit system performance.
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Page 35
Operation
CHAPERONE® BED EXIT WITH ZONE CONTROL (OPTIONAL)
“Zone 1” LED
1. Before positioning the patient on the bed, the scale system must be zeroed for the Bed Exit System to function
properly (see page 37 for instructions on zeroing the scale system).
2. Position the patient on the bed and press the “Arm/Disarm” button to activate the Bed Exit function. The footboard
“Zone 1” LED and indicator “Bed Exit” LED will turn on.
3. The Bed Exit system with Zone Control automatically selects Zone 1. To change the Zone, press and hold the
“Zone” button until the light indicating the desired Zone comes on.
4. To deactivate Bed Exit, press the “Arm/Disarm” button. The selected footboard Zone light and the indicator “Bed
Exit” lights will turn off.
NOTE
Moving the litter position after Bed Exit is armed may trigger the alarm.
WARNING
To avoid possible injury and to assure proper operation when using a powered mattress replacement system such as
XPRT, do not initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and
position resulting from a dynamic therapy mattress may adversely affect bed exit system performance.
Chaperone® Zone Settings
The first zone (left indicator light) is the traditional Bed Exit zone. The patient can move around the bed freely but
cannot fully exit the bed or the alarm will sound.
The second zone (middle indicator light) is more restrictive than the first zone. When the zone is selected, the bed
measures the location of the patient’s center of gravity. If the patient’s center of gravity moves from the original
location more than 6.5 inches to either side or 13 inches toward the head or foot, an alarm will sound.
The third zone (right indicator light) is the most restrictive zone. When the zone is selected, the bed measures the
location of the patient’s center of gravity. If the patient’s center of gravity moves from the original location more than
1 inch to either side or 1 inch toward the head or foot, an alarm will sound.
NOTE
All zone dimensions are ± .5 inches.
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Page 36
Operation
SCALE SYSTEM (OPTIONAL)
Weighing a Patient on the Scale System
The scale feature provides information to the caregiver on the weight of a patient.
To Weigh a Patient:
1. Press and hold the (“Scale”) button.
2. “Release Button” message flashes on the display as shown in figure 40.
3. Release the “Scale” button.
4. After the “Scale button has been released, “Weighing ... Do Not Touch
Bed” message will flash on the display as shown in Figure 41.
5. When weighing has been completed, the patient’s weight will be displayed
on the status screen as shown in Figure 42. The patient weight displayed is
stored in the system for later use.
NOTE
• Pressing the scale button again within 60 seconds of the first press (this
means that the scale data is still being displayed on the status screen), will
remove the data from the screen. This second button press will remove the
data so that the operator can walk away and not worry about having the data
available to non authorized persons. The second button press will not log a
value into the weight log. If the operator would like to have two consecutive
readings within 60 seconds, then the operator will need to press the button
once for the first weight reading, a second time will remove the weight information from the display and then a third time to take another weight reading
• If weight is displayed the “Scale” button can be pressed to turn off the scale.
Figure 40
Figure 41
Figure 42
CAUTION
Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse
Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the potential
for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full down position
to prevent the interference from causing the scale system to weigh inaccurately.
WARNING
To avoid possible injury and to assure proper operation when using a powered mattress replacement system such as
XPRT:
• Confirm proper scale system operation following mattress installation. For best results, secure the mattress power
cord to prevent damage to the cord and interference with the bed frame and the scale system.
• Do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn Assist active. Patient motion
and position resulting from the dynamic therapy mattress may adversely affect scale system performance.
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Page 37
Operation
SCALE SYSTEM (OPTIONAL)
Zeroing The Scale System
This feature provides the operator to zero the bed prior to weighing patient. Do not zero the bed while a patient is in
the bed. If this should occur, remove the patient and zero the bed again. If the Bed Exit is armed, you must disarm it
before the scale can be zeroed.
To Zero the Bed:
1. Press and hold the (“Zero”) button.
2. “Hold to Zero Bed” message will appear briefly on the display as shown in
figure 43.
3. Immediately following the “Hold to Zero Bed” message, the “Release
Button” message will flash on the display as shown in Figure 44.
4. Release the “Zero” button.
5. After the “Zero” button has been released, “Do Not Touch Bed” message
will flash on the display as shown in Figure 45.
6. When zeroing has been completed:
a. “Zeroing Successful” message will be shown on the display as shown
in Figure 46.
b. The Bed Zero LED will illuminate.
c. The display will show the status screen with the scale information as
shown in Figure 47.
7. The bed is now ready for the patient.
Figure 43
Figure 44
Figure 45
Figure 46
Figure 47
NOTE
If there is a problem with a load cell or another component of the scale system, the system will try to zero up to 30
seconds, after which the scale monitor will read: “Unable to Zero - Try Again” if unsuccessful.
If the problem continues after three attempts, the scale system will lock and the scale monitor will read: “Unable to
Zer o”.
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Page 38
Operation
MENU
• The Main Menu screen contains selectable product features to the caregiver. There are eight features listed in
the main menu as ordered below:
1. Weight Log (Weight Log is the Default Selection) 5. Scale Units (Change Scale Units)
2. Gain/Loss 6. Backlight (Backlighting)
3. Change Equip. (Change Equipment) 7. Advanced Options
4. Change Ptnt. Wgt. (Change Patient Weight) 8. Exit Menu
• To select a feature, press the “Menu Up” and “Menu Down” button to scroll to the desired feature. Highlight the
desired feature to select and then press the “Enter” button.
1. Weight Log
This feature provides the operator up to 10 of the last weights logged by the scale system as shown in Figure 3.
To display a list of the previous 10 weight readings:
• Press the “Menu” button and select the item “Weight Log”.
• Press the “Up” or “Down” buttons to scroll through the weight log.
• A weight reading is logged each time the scale button is pressed
and the bed is in the scale mode for at least 15 seconds.
• The first weight reading displayed (1.) is the most recent. If the
change in the patient’s weight since the last reading was taken
is less than .2 pounds, the log will not update. Zeroing the scale
system clears the weight log.
Figure 3
2. Gain/Loss
This feature provides information to the caregiver on the weight gain or
loss of the patient.
To e nable:
• Select “Gain/Loss” in the menu then press the “Enter” button, Figure
4 will be displayed.
• When “Release Button” message flashes on the display, release
the “Enter” button; “Do Not Touch Bed” message will flash on the
display.
• When Gain/Loss is On, “Gain/Loss Enabled” message displays.
NOTE: Refer to Figure 5
• The base represents the scale weight when the gain/loss feature
was enabled.
• The second piece of information represents the “Gain” or the “Loss”
and the weight difference between the current displayed weight and
the saved base weight.
NOTE: Refer to Figure 6
• If the Gain or the Loss exceeds 99.9 lb, then the system will display
‘---’ instead of a value.
Figure 4
Figure 5
Figure 6
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Page 39
MENU (CONTINUED)
Hold to
Change Equipment
Equipment
Changed
Hold to Change
Patient Weight
3. Change Equipment
The change equipment feature allows the operator to add or remove item
from the product without affecting the patient weight.
To Change Equipment:
• Select “Change Equip.” in the menu then press the “Enter” button,
Figure 7 will be displayed or if the operator did not press the button
long enough the message “Hold Button Longer” will appear in the
message window.
• When “Release to Start” message displays on the screen, release
the “Enter” button; “Do Not Touch Bed” message will flash on
display.
• Figure 8 will display when the system is ready to change equipment.
• Press the “Enter” button to Add/Remove equipment or press the
“Exit” button to cancel operation.
• If “Enter” is pressed to Add/Remove Equipment then the
message “Do Not Touch Bed” will flash on the display.
• If “Exit” is pressed, “Operation Canceled” message will display.
• Figure 9 will be displayed when the system completes the change
equipment adjustment.
• The status screen will then display the weight of the patient only.
Operation
Figure 7
Figure 8
4. Change Patient Weight
The change patient feature allows the operator to add or remove weight from the patient weight.
To C hange Patient Weight:
• Select “Change Pnt. Wgt.” in the menu.
• Press and hold the “Enter” button, Figure 10 will be displayed.
• When “Release Button” message displays on the screen, release
the “Enter” button; “Do Not Touch Bed” message will flash on
display.
• When the system is ready to change patient weight the following
information will be displayed:
- Allow used to Change patient Weight using arrow button;
- Display the new patient weight;
- Press” Enter” when done;
- Press “Exit” to cancel operation.
• If “Enter” is pressed, the message “Do Not Touch Bed” will flash on the display.
• If “Exit” is pressed, “Patient Weight Changed” message will display.
Figure 10
Figure 9
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Page 40
MENU (CONTINUED)
5. Scale Units
• The Change Scale Units feature allows the operator to select the
unit of value (lb or kg) for the scale information that is presented on
the display.
• When the change scale units is selected, Figure 11 is displayed.
• This screen will highlight the current scale unit setting.
• To change the scale unit setting, scroll to the desired setting and
press the “Enter” button.
• The default setting is “lb”
6. Backlight
• When the backlight feature is selected the display will change to the
backlight selection screen as shown in Figure 12.
• This screen will highlight the current backlight setting.
• Five settings are available for the backlight; Off, Low, Medium, High
and Nurse Call Only.
• To change the backlight setting; scroll to the desired setting and
press the “Enter” Button; “Save Successful” message will display.
• The default setting is “Low”.
Operation
Fig ure 11
Figure 12
7. Advanced Options
The advanced menu items include:
1. Choose Exit Alarm
2. Brake Alarm
3. Awareness Alarm
4. Status To Nurse Call
Advanced Options: Choose Exit Alarm
The caregiver can choose between 10 exit alarms.
To Select Alarm:
• Select “Choose Exit Alarm” from the menu.
• Scroll through the 10 Tone Patterns listed in the menu. A sample alarm will sound for each Tone Pattern
highlighted.
• Select desired Tone Pattern and Press “Enter”
• “Save Successful” message will be displayed.
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Page 41
MENU (CONTINUED)
Advanced Options: Brake Alarm
The caregiver can enable or disable an audible brake alarm feature. If enabled and the brakes are not
engaged when the bed is plugged in, an audible alarm will occur.
To Enable/Disable Brake Alarm:
• Select “Brake Alarm” from the menu.
• Use the Up and Down Arrow buttons to select enable or disable the alarm.
• Press “Enter” to save the alarm state.
• “Save Successful” message will be displayed.
Advanced Options: iBed® Awareness Alarm (Audible)
The caregiver can enable or disable an audible alarm for iBed® Awareness alert states.
To Enable/Disable Alarm:
• Select “Awareness Alarm” from the menu.
• Select “On” to Enable or “Off” to disable and then press “Enter”
• “Save Successful” message will be displayed.
Operation
Advanced Options: Status Nurse Call (iBed® Awareness Priority Signal)
The caregiver can enable or disable a priority signal alarm through the Nurse call system based on an iBed
Awareness alarm state.
To Enable/Disable Alarm:
• Select “Status To N/C” from the menu.
• Select “On” to Enable or “Off” to disable and then press “Enter”
• “Save Successful” message will be displayed.
8. Exit Menu
Exits Main Menu screen and returns display to the default Status Screen.
®
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Page 42
Operation
iBED® AWARENESS INTENDED USE
The iBed® Awareness system is intended to serve as a secondary monitoring system, informing the operator via a visual
or audible alert when a preset condition changes.
• When the iBed® Awareness is turned “On”, the system has the ability to automatically monitor the following:
- Brake Set/Not Set
- Siderail Position
• Additionally, when the bed is in low height and/or Chaperone® Bed Exit with Zone Control system is armed and/or
the Fowler 30+ is “On”, the system has the ability to monitor these features independently when iBed® Awareness
is turned “On”.
iBED® AWARENESS FUNCTIONALITY
• The i Bed® Awareness provides functionality that will monitor status conditions on the product and produce an alert
if the state had changed.
• When the system is turned “On”, it monitors each of the siderail positions and brake automatically. If the bed is in
Low Height and/or the Bed Exit is armed and/or the Fowler 30
features when iBed® Awareness is turned “On”.
NOTE: If the Fowler 300+ lock is “On” before iBed® Awareness is “On”, the system will also
monitor the Fowler 300+ lock.
• In the event of a power loss, the iBed® Awareness system will store the last known condition and when power is
restored it will operate in this condition.
• iBed® Awareness will not be able to be turned “On” if any system error conditions exist that impede the function of
the iBed® Awareness system. The system errors that affect this feature include the four siderail sensors, the scale
system, the Fowler 300 + lock and the bed exit system. For details on error codes, refer to the Maintenance Manual.
0
+ lock is “On”, the system will also monitor these
iBED® AWARENESS LIGHT BAR AND SIDE LIGHTS
A light bar, located centrally on the front of the footboard, will illuminate and indicate the state of the iBed
Awareness system. Side lights located on the sides of the footboard will behave identical to the center light.
Features
• When the iBed® Awareness system is “On” the light bar turns green.
• If an alert state on the iBed® Awareness system is triggered, the light bar will change to the alert state and
flash AMBER.
• During an alert state, an AMBER LED associated with the alert will blink on the footboard and the display
screen will show the details of the alert state.
iBED® AWARENESS ON/OFF BUTTON
TheOn/Off control button is used to turn the iBed® Awareness system “On” and “Off”.
Features
When the button is pressed the iBed® Awareness system will save information based on the current state of the
product and based on the system rules will commence monitoring.
Turning on the iBed® Awareness system
1. Press the iBed On/Off button.
2. The following message will be displayed on the screen: “Awar eness On”.
Turning off the iBed® Awareness system
1. Press and hold the iBed On/Off button.
2. The following message will be displayed on the screen: “Awareness Off”.
®
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Page 43
Operation
iBED® AWARENESS MONITORING AND ALARMS
Low Height
• If the low height state changes:
1. The low height LED blinks and the display screen flashes between the message in Figure 13 and the
message in Figure 14.
Figure 13
Figure 14
Brakes
• If the brake state changes:
1. The brake LED blinks and the display screen flashes between the message in Figure 15 and the message
in Figure 16.
Figure 15
Figure 16
Siderails
• If the siderail state changes:
1. The siderail LED blinks and the display screen flashes between the message in Figure 17 and the message in Figure 18.
Figu re 17
Figure 18
NOTE
The arrow pointing to the siderail in Figure 17 and 18 will change depending on the siderail position in alarm.
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Page 44
Operation
iBED® AWARENESS MONITORING AND ALARMS (CONTINUED)
Bed Exit
• If the bed exit is disarmed:
1. The bed exit LED blinks and the display screen flashes between the message in Figure 19 and the message in Figure 20.
Figure 19
0
Fowler 30
• If the fowler 300+ lock state changes from a locked to an unlocked state:
1. The fowler 300+ lock LED blinks and the display screen flashes between the message in Figure 21 and
• If the fowler 300+ lock state changes to a lowered position:
1. The fowler 300+ lock LED blinks and the display screen flashes between the message in Figure 23 mes-
+ Lock
the message in Figure 22.
Figure 21
sage and the message in Figure 24.
Figure 20
Figure 22
Figure 23
Figure 24
Additional Alarm Conditions
• If an audible alarm is required, the caregiver can set the Awareness alarm to “On” through the Advanced
Options Menu in the Main Menu.
• If the caregiver would like to set the Awareness alarm to the Nurse Call Station, the “Status To N/C” must be
turned “On” through the Advanced Options Menu in the Main Menu.
NOTE
• By default these two advanced options are turned “Off”.
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Page 45
Operation
iBED® AWARENESS LOCKS
Fowler 300+ Lock button
• The Fowler 300+ lock is a dual purpose button. It positions the Fowler to
300 and removes the bed out of trend.
• When the Fowler 300+ lock button is pressed, the bed will reposition if it
needs to and Figure 25 will be displayed.
• Once the bed reaches its final position, Figure 26 will be displayed.
• If the button is not held until the final position is reached Figure 27 will be
displayed.
• If bed is put in CPR position manually or by pressing the CPR button,
Figure 28 will be displayed.
• If the bed is at its final fowler 300+ position (Trend = 00, fowler = 300) and the user presses either the fowler
down or trend buttons, the display will toggle between figures 31 and 32.
Figure 25
Figure 26
Bed Motion Lock
• If Bed Motion lock button is
pressed, Figure 29 will be
displayed.
• If Bed Motion lock button is
pressed when already “on” then
Figure 30 will be displayed.
• If Motion is attempted when
lock is “On,” the display screen
flashes between Figure 31 and
32.
NOTE: The CPR Drop button overrides all locks.
Figure 27
Figure 29 Figure 30
Figure 31
Figure 28
Figure 32
Patient Control Locks
• If any of the Patient Control lock buttons are pressed, Figure 29 as shown above will be displayed.
• If any of the Patient Control lock buttons are pressed when already “on” then Figure 30 as shown above will
be displayed.
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Page 46
PENDANT - MOTION/NURSE CALL
(3006-315-011)
Operation
Press to activate Nurse Call.
Press to raise head section.
Press to lower head section.
PENDANT - MOTION/NURSE CALL/SMART TV (DIGITAL)
(3006-315-012)
Press to turn on/off the TV.
Press to increase the volume
of the TV.
Press to raise knee section.
Press to lower knee section.
Press to activate Nurse Call.
Press to change to a higher
numbered channel.
Press to decrease the volume
of the TV.
Press to raise head section.
Press to lower head section.
Press to turn on/off room lights
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Press to change to a lower
numbered channel.
Press to raise knee section.
Press to lower knee section.
Press to turn on/off reading lights
Page 47
OPTIONAL INFRARED (IR) MODULE
1
Operation
2
Item Name Function
IR (Infrared) Module Cable
1
IR (Infrared) Lens
2
iBed Locator Connection LED
3
Wireless (WiFi) Connection LED
4
Connects to the bed and provides power and signal
communications.
Provides infrared communications with the iBed
Locator.
Provides connection status for IR (infrared)
communications with iBed Locator.
Slow Flash - attempting to connect to iBed Locator.
Solid LED - iBed Locator connected.
Rapid Flash - Error condition detected.
OFF - iBed Locator is not trying to connect.
Provides connection status for WiFi (wireless)
communications with wireless access point.
Slow Flash - WiFi attempting to connect.
Solid LED = WiFi connected.
Rapid Flash - WiFi was not connected after 6 minutes
and timed out.
3 4
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Page 48
Operation
OPTIONAL IBED LOCATOR
The Optional iBed Locator component provides iBed Locator ID and battery status information to the IR Module.
Installation and operational procedures for the Optional iBed Locator are located in the i Bed Locator Instructions For
Use manual (5212-00 9-101).
1
Item Name Function
IR (Infrared) Lens Provides Infrared communications with the iBed IR Module.
1
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Page 49
Preventive Maintenance
At a minimum, check all items listed during annual preventive maintenance for all Stryker products. You may need to
perform preventive maintenance checks more frequently based on your level of product usage.
CHECKLIST
____ _ All fasteners secure (reference all assembly drawings).
__ ___ Engage brake pedal and push on the bed to ensure all casters lock securely.
__ ___ Inspect the brake assembly (Brake Ratchet Spring and Brake Bar) for degradation or signs of wear at the
foot end and head end of the bed. Ensure brake assembly components (locking caster and springs) are
functioning properly.
__ ___ “Brake” LED on the footboard and head end siderails blink when brakes are not engaged.
____ _ Locking steer caster engages and disengages properly.
__ ___ Siderails move, latch and stow properly.
__ ___ CPR release working properly.
__ ___ Foot prop intact and working properly.
__ ___ I.V. pole working properly.
__ ___ Foley bag hooks intact.
__ ___ No cracks or splits in headboard, footboard or siderail panels.
__ ___ No rips or cracks in mattress cover.
__ ___ All functions on head end siderails working properly (including LEDs).
__ ___ All functions on footboard working properly (including LEDs).
__ ___ Scale and Bed Exit system calibrated properly.
__ ___ Motion Interrupt switches working properly.
__ ___ Night light working properly.
__ ___ Power cord and plug not frayed or damaged.
__ ___ No cables worn or pinched.
__ ___ All electrical connections tight.
__ ___ All grounds secure to the frame.
__ ___ Ground impedance not more than 200 mΩ (milliohms).
__ ___ Current leakage not more than 300 μA (microamps).
__ ___ Apply grease to the Litter grease points (see Maintenance manual for locations).
__ ___ Ensure ground chains are clean, intact, and have at least two links touching the floor.
__ ___ Check Fowler angle for accuracy 00 - 600.
__ ___ Check that the fowler holds its position at 300 with patient weight.
__ ___ Siderail switches working properly (iBed® Awareness option).
__ ___ Center Light Bar LED and side light LED working properly (iBed® Awareness option).
__ ___ Inspect footboard control labeling for signs of degradation.
__ ___ Inspect siderail gas spring for oil leaks and replace if necessary.
__ ___ Inspect fowler damper for oil leaks and replace if necessary.
__ ___ Check all motion functionality.
____ _ Check Nurse Call functionality.
____ _ Check Nurse Call battery - optional equipment.
_____ Confirm iBed® Wireless Module and IR Module are intact and footboard icons are displaying
(iBed® Wireless Option).
Bed Serial Number:
Completed by: _______________________________________ Date: ___________________
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Page 50
Cleaning
CAUTION
Always unplug the power cord during service or cleaning.
Hand wash all surfaces of the bed with warm water and mild detergent. DRY THOROUGHLY. Do not steam clean or
hose off the S3® MedSurg Bed, Model 3005. Do not immerse any part of the bed. Some of the internal parts of the
bed are electric and may be damaged by exposure to water.
Suggested cleaners for bed surfaces:
• Quaternary Cleaners (active ingredient − ammonium chloride)
• Phenolic Cleaners (active ingredient − o−phenylphenol)
• Chlorinated Bleach Solution (5.25% − less than 1 part bleach to 100 parts water)
Avoid over saturation and ensure the product does not stay wet longer than the chemical manufacturer’s guidelines
for proper disinfecting.
CAUTION
• Some cleaning products are corrosive in nature and may cause damage to the product if used
improperly. If the products described above are used to clean Stryker patient care equipment, measures
must be taken to insure the beds are wiped with a damp cloth soaked in clean water and thoroughly
dried following cleaning. Failure to properly rinse and dry the beds will leave a corrosive residue
on the surface of the bed, possibly causing premature corrosion of critical components. Failure to
follow the above directions when using these types of cleaners may void this product’s warranty.
• Do not use quaternary disinfectants formulated with Glycol Ethers.
For mattress cleaning instructions, please see the tag on the mattress, or contact the mattress manufacturer.
Clean Velcro AFTER EACH USE. Saturate Velcro with disinfectant and allow disinfectant to evaporate. (Appropriate
disinfectant for nylon Velcro should be determined by the hospital).
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Page 51
EMC Information
S3® MEDSURG BED, MODEL 3005
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
The S3® MedSurg Bed, Model 3005 is suitable for use in the electromagnetic environment specified below. The
customer or the user of the S3® MedSurg Bed, Model 3005 should assure that it is used in such an environment.
Immunity Test IEC 60601 Test Level Compliance Level
Electrostatic Discharge (ESD)
IEC 61000-4-2
Electrostatic fast
Transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, voltage variations
and short interruptions on
power supply input lines
IEC 61000-4-11
Power frequency (50/60 Hz)
magnetic field
IEC 61000-4-8
Note: UT is the a.c. mains voltage prior to applications of the test level.
+6 kV contact
+8 kV air
+2 kV for power
supply lines
+1 kV for input/
output lines
+8 kV differential mode
+2 kV common mode
<5%Ut (95% dip in Ut) for
0.5 cycle
40%Ut (60% dip in Ut) for
5 cycles
70%Ut (30% dip in Ut) for
25 cycles.
<5% Ut (>95% dip in Ut)
for 5 sec.
3 A/m 3 A/m Power frequency magnetic
+6 kV contact
+8 kV air
+2 kV for power
supply lines
+1 kV for input/
output lines
+8 kV differential mode
+2 kV common mode
<5%Ut (95% dip in Ut)
for 0.5 cycle
40%Ut (60% dip in Ut)
for 5 cycles
70%Ut (30% dip in Ut)
for 25 cycles.
<5% Ut (>95% dip in Ut)
for 5 sec.
Electromagnetic
Environment Guidance
Floors should be wood,
concrete, or ceramic tile. If
floors are covered with synthetic
material, the relative humidity
should be at least 30%.
Main power quality should be
that of a typical commercial or
hospital environment.
Main power quality is that of
a typical commercial and/or
hospital environment.
Main power quality should be
that of a typical commercial
and/or hospital environment. If
the user of the S3® MedSurg
Bed, Model 3005 requires
continued operation during
power main interruptions,
it is recommended that the
device be powered from an
uninterrupted power supply or
a battery.
fields should be at levels
characteristic of a typical
location in a typical commercial
and/or hospital environment.
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Page 52
EMC Information
S3® MEDSURG BED, MODEL 3005 (CONTINUED)
Recommended separation distances between portable and mobile RF
communications equipment and the S3® MedSurg Bed, Model 3005.
The S3® MedSurg Bed, Model 3005 is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the S3® MedSurg Bed, Model 3005 can help prevent
electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications
equipment (transmitters) and the S3® MedSurg Bed, Model 3005 as recommended below, according to the maximum
output power of the communications equipment.
Rated maximum output
power of transmitter
W
150 kHz to 80 MHz
0.01 1.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
Separation distance according to frequency of transmitter
m
80 MHz to 800 MHz
d=1.2
d=1.2
8000 MHz to 2.5 GHz
d=2.3
10 3.8 3.8 7. 3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
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Page 53
EMC Information
S3® MEDSURG BED, MODEL 3005 (CONTINUED)
The S3® MedSurg Bed, Model 3005 is suited for use in the electromagnetic environment specified below. The
customer or the user of the S3® MedSurg Bed, Model 3005 should assure that it is used in such an environment.
Immunity Test IEC 60601 Test Level
Conducted
RF
3 Vrms
150 kHz to 80 MHz
IEC 61000-4-6
Compliance
Level
3 Vrms
Electromagnetic Environment - Guidance
Portable and mobile RF communications
equipment should be used no closer to any
part of the S3® MedSurg Bed, Model 3005,
including cables, than the recommended
separation distance calculated from the
equation appropriate for the frequency of the
transmitter.
Recommended Separation Distance
d=1.2
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d=1.2
d=2.3
800 MHz to 2.5 GHz
where Pis the maximum output power rating
of the transmitter in watts (W) according to
the transmitter manufacturer and dis the rec-
ommended separation distance in metres (m).
Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
survey,a should be less than the compliance
level in each frequency range.
b
Interference may occur in the vicinity of
equipment marked with the following symbol:
Note 1
At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location in which the S3® MedSurg Bed, Model 3005 is
used exceeds the applicable RF compliance level above, the S3® MedSurg Bed, Model 3005 should be observed
to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the S3® MedSurg Bed, Model 3005.
b
Over the frequency range 150 kHz to 80 MHz, field strengths are less than 3 V/m.
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Page 54
EMC Information
S3® MEDSURG BED, MODEL 3005 (CONTINUED)
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
The S3® MedSurg Bed, Model 3005 is intended for use in an electromagnetic environment specified below. The
customer or the user of the S3® MedSurg Bed, Model 3005 should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment
Group 1,
RF Emissions
CI S P R 11
RF Emissions
CI S P R 11
without iBed®
Wireless option
Group 2,
with iBed®
Wireless option
Class A
The S3® MedSurg Bed, Model 3005 uses RF energy only
for its internal function. Therefore, its RF emissions are
very low and are not likely to cause any interference in
nearby electronic equipment.
The S3® MedSurg Bed, Model 3005 is suitable for use in
all establishments other than domestic and those directly
connected to the public low voltage power supply network
that supplies buildings used for domestic purposes.
Harmonic Emissions
IEC 61000-3-2
Voltage Fluctuations
Flicker Emissions
IEC 6100-3-3
Class A
Complies
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Warranty
LIMITED WARRANTY
Stryker Medical Division, a division of Stryker Corporation, warrants to the original purchaser the S3® MedSurg Bed,
Model 3005 to be free from defects in material and workmanship for a period of one (1) year after date of delivery.
Stryker’s obligation under this warranty is expressly limited to supplying replacement parts and labor for, or replacing,
at its option, any product which is, in the sole discretion of Stryker, found to be defective. If requested by Stryker,
products or parts for which a warranty claim is made shall be returned prepaid to the factory. Any improper use or
any alteration or repair by others in such manner as in Stryker’s judgment affects the product materially and adversely
shall void this warranty. Any repair of Stryker products using parts not provided or authorized by Stryker shall void this
warranty. No employee or representative of Stryker is authorized to change this warranty in any way.
Stryker Medical Bed products are designed for a 10 year expected service life under normal use, conditions, and with
appropriate periodic maintenance as described in the maintenance manual for each device. Stryker warrants to the
original purchaser that the welds on its Bed products will be free from structural defects for the expected 10 year life
of the Bed product as long as the original purchaser owns the product.
Stryker Medical optional components and/or accessories are warranted as follows:
• Motion/Nurse Call Pendant: Two (2) years service life under normal use and proper care
• Motion/Nurse Call/SmartTV Pendant: Two (2) years service life under normal use and proper care
• iBed® Wireless Components: Ten (10) years service life under normal use and proper care
WARRANTY EXCLUSION AND DAMAGE LIMITATIONS
The express warranty set forth herein is the only warranty applicable to the product. Any and all other warranties,
whether express or implied, including any implied warranty of merchantability or fitness for a particular purpose are
expressly excluded by Stryker. In no event shall Stryker be liable for incidental or consequential damages.
TO OBTAIN PARTS AND SERVICE
Stryker products are supported by a nationwide network of dedicated Stryker Field Service Representatives. These
representatives are factory trained, available locally, and carry a substantial spare parts inventory to minimize repair
time. Simply call your local representative or call Stryker Customer Service at 1-800-327 -0770.
RETURN AUTHORIZATION
Product cannot be returned without prior approval from the Stryker Customer Service Department. An authorization
number will be provided which must be printed on the returned product. Stryker reserves the right to charge shipping
and restocking fees on returned product. Special, modified, or discontinued products are not subject to return.
DAMAGED MERCHANDISE
ICC Regulations require that claims for damaged product must be made with within fifteen (15) days of receipt of the
product. Do not accept damaged shipments unless such damage is noted on the delivery receipt at the time of receipt.
Upon prompt notification, Stryker will file a freight claim with the appropriate carrier for damages incurred. Claims will
be limited in amount to the actual replacement cost. In the event that this information is not received by Stryker within
the fifteen (15) day period following the delivery of the product, or the damage was not noted on the delivery receipt at
the time of receipt, the customer will be responsible for payment of the original invoice in full within thirty (30) days of
receipt. Claims for any incomplete shipments must be made within thirty (30) days of invoice.
INTERNATIONAL WARRANTY CLAUSE
This warranty reflects U.S. domestic policy. Warranty outside the U.S. may vary by country. Contact your local Stryker
Medical representative for additional information.
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Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
2016/06 3005-009-001 REV G www.stryker.com
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